Method and composition for improved anabolism

ABSTRACT

Nutritional compositions are provided containing at least one PPAR agonist, at least one PGC-1alpha agonist, and at least one creatine derivative. Methods of promoting anabolism and improving or enhancing physical performance using the compositions are provided. The compositions and methods can be combined with physical training or exercise.

This application claims the benefit of earlier filed U.S. Provisional Patent Application Ser. No. 61/259,633 filed on Nov. 9, 2009.

FIELD OF THE INVENTION

A composition that, through the stimulation of peroxisome proliferator-activated receptors (PPARs) and peroxisome proliferator-activated receptor-γ coactivator (PGC-1α) during training, regulates athletic function and stimulates the anabolic pathway is provided. The composition may be utilized as a dietary supplement or conventional food to improve athletic function and/or muscle growth and development via improved anabolism.

BACKGROUND

Anabolism is a key factor in the process of muscle growth for athletes and body builders. Anabolism is comprised of multiple metabolic pathways, constructing larger molecules from their building blocks. Energy is a necessary part of these metabolic pathways. In contrast, catabolism is the deconstruction of large molecules into smaller ones. Anabolism is fueled by both the small molecules of catabolism as well as an energy source, such as, but not limited to, adenosine triphosphate (ATP). The anabolic process and related anabolic hormones stimulate protein synthesis and muscle growth.

Anabolic reactions are synthesis reactions and are endergonic, meaning that they consume more energy than they produce. Anabolism is the process of chemical reactions that combine simple molecules and monomers to form the body's complex structural and functional components. Glucose may take part in or be formed via several anabolic reactions such as, for example, synthesis of glycogen or the synthesis of new glucose molecules from byproducts of protein and lipid breakdown, i.e., gluconeogenesis.

One way of promoting anabolism is through the use of a dietary supplement or drug. However, many anabolic stimulation compositions are illegal or have been banned from use by athletes in a number of professional, collegiate, and amateur sports. Additionally, anabolic stimulating products also generally tend to have undesired side effects that can be harmful to the health of an individual. Thus, there is a need and a demand for a dietary ingredient or composition which can promote anabolism without undesirable side effects and/or which is suitable for use by athletes.

For the most part, anabolism is increased where there is an energy source and a way to synthesize proteins and therefore build new muscle. One energy source is ATP. Alternative energy sources include compounds or methods to increase metabolism. The ability and rate at which the body can spare and replenish energy is critical for anabolism.

Peroxisome proliferator-activated receptors (PPARs) are nuclear receptor protein transcription factors that operate to regulate the expression of genes. PPARs have been identified in a wide variety of human tissue and play an essential role in the regulation of processes such as cellular differentiation, development, and metabolism. The oral use of ingredients which increase the activity of PPARs is one approach to fostering anabolism and regulating athletic function.

Peroxisome proliferator-activated receptor-γ coactivator (PGC)-1α (“PGC-1alpha”) regulates energy metabolism and promotes mitochondrial biogenesis. Mitochondria convert nutrients into energy. While exercise alone is enough to increase the expression of PGC-1alpha, exercise plus known activators of PGC-1alpha may work together to regulate energy metabolism and promote mitochondrial biogenesis, thereby stimulating anabolism. The oral use of ingredients which affect the synthesis or activity of PGC-1alpha in dietary supplements is another approach to fostering anabolism and regulating athletic function.

A transcription coactivator is defined as a protein or protein complex that increases the probability of a gene being transcribed by interacting with transcription factors but does not itself bind to DNA in a sequence-specific manner. The PPARs are members of a relatively large family of nuclear receptors, all of which are subject to transcriptional coactivation by PCG-1 alpha (Liang, et al., Advan. Physiol. Edu. (2006) 30:145-151).

In view of the above, there is a need and a desire for a dietary supplement including or containing ingredients that help regulate PGC-1alpha and PPARs to foster anabolism and regulate athletic function.

SUMMARY OF THE INVENTION

The presently claimed invention relates to a method for the stimulation of anabolism and, more particularly, the administration to an individual of an effective amount of at least one compound that has an effect on PPAR and at least one compound which has an effect on PGC-1 alpha to enhance or increase anabolic processes in a human subject.

The object of the invention can be obtained, at least in part, by administering to an individual (i.e., a human) a nutritional composition including or containing ingredients that help regulate PGC-1alpha and PPARs to promote greater anabolism. The PGC-1alpha and PPAR regulating sources can be administered alone or in conjunction with compounds that promote muscle formation, promote protein synthesis, stimulate the metabolism or help regulate other hormones that are essential to anabolism.

In accordance with one embodiment, the nutritional composition comprises at least one PPAR agonist and at least one PGC-1alpha agonist.

In accordance with another embodiment, the nutritional composition consists essentially of at least one PPAR agonist and at least one PGC-1alpha agonist.

In a further embodiment, the nutritional composition consists of at least one PPAR agonist and at least one PGC-1alpha agonist.

In a still further embodiment, the nutritional composition can comprise, consist essentially of, or consist of at least one compound that has an effect on PPAR, PGC-1alpha, or both and at least one creatine derivative or creatine containing compound.

In accordance with certain other embodiments, the nutritional composition can further include central nervous system stimulants and/or an energy source to promote protein synthesis and/or increase metabolism.

In accordance with other embodiments, a method for providing a beneficial physical effect can comprise administering to an individual (i.e., a human subject) a therapeutically effective amount of a nutritional composition which comprises, consists essentially of or consists of at least one PPAR agonist and at least one PGC-1alpha agonist. The beneficial physical effect can be improved, enhanced or increased muscle growth, anabolism, anti-catabolism, strength, recovery, endurance, and/or mental focus, mood elevation, improved insulin resistance, increased nitric oxide production, and/or improved energy metabolism.

In accordance with further embodiments, a method for enhancing physical performance can comprise administering to an individual a therapeutically effective amount of a nutritional composition which comprises, consists essentially of or consists of at least one PPAR agonist and at least one PGC-1alpha agonist. Enhanced physical performance includes, for example, improved or enhanced anabolism, anti-catabolism, anti-fatigue, strength, endurance, mental focus, and/or recovery when combined with exercise.

The methods disclosed herein contemplate the administration of a nutritional composition which can provide an improvement in anabolism in comparison to other pre-training, during-training, or post-training compositions. Suitably, the nutritional compound promotes anabolism without unwanted and potentially dangerous side effects generally associated with other products, such as anabolic steroids, that promote anabolism.

As used herein it is understood that the term “creatine containing” may also include derivatives and analogues of creatine and salts or esters thereof.

As used herein it is understood that the term “PGC-1” may include PGC-1α, PGC-1β, PGC-1δ and PGC-1γ. Also contemplated herein for use in the nutritional compositions are PGC-1 agonists, antagonists, and derivatives, conjugates, and salts thereof.

As used herein it is understood that the term “PPAR” may include all peroxisome proliferator-activated receptors, and isoforms thereof. Also contemplated herein for use in the nutritional compositions are PPAR agonists, antagonists, and derivatives, conjugates, and salts thereof.

DETAILED DESCRIPTION

Anabolism is comprised of multiple metabolic pathways, constructing larger molecules from their building blocks. Energy is a necessary part of these metabolic pathways. In contrast, catabolism is the deconstruction of large molecules into smaller ones. Anabolism is fueled by both the small molecules of catabolism as well as an energy source, such as, but not limited to, adenosine triphosphate (ATP). The anabolic process and related anabolic hormones stimulate protein synthesis and muscle growth.

The object of the presently claimed invention can be obtained, at least in part, by administering to an individual (i.e., a human subject) an effective amount of a nutritional composition including one or more ingredients that help regulate PGC-1alpha and/or PPARs. The PGC-1alpha and PPAR regulating sources can be administered alone or in conjunction with compounds that promote muscle formation, promote protein synthesis, stimulate the metabolism, or regulate other hormones that are essential to anabolism.

In accordance with one embodiment, a method for promoting anabolism includes administering to an individual an effective amount of a nutritional composition including PGC-1alpha and PPAR regulators. The PGC-1alpha and PPAR regulating compounds act to induce activity of the PGC-1alpha and PPARs and are agonists.

PPARs are lipid-activated transcription factors that belong to the steroid/thyroid/retinoic acid receptor superfamily. All of their characterized target genes encode proteins that participate in lipid homeostasis. Certain PPARs induce the expression of many genes involved in lipid anabolism. PPARs stimulate anabolic processes such as adipogenesis, lipogenesis and glucose uptake. PPARs also act as nutritional sensors that regulate a variety of homeostatic functions including metabolism, inflammation and development. PPAR-gamma (PPAR-γ) regulates anabolism or storage. The equilibrium between anabolic and catabolic processes is under the control of chondrocytes, which are under the influence of PPARs. PPARs act by dimerizing with receptors that then bind to specific regulatory regions on the DNA of target genes, called peroxisome proliferator response elements (PPREs). When the PPARs (and associated proteins in the PPRE complex) bind to the genes, transcription of the target genes is then increased or decreased, depending on the gene. PPARs bind specific ligands and regulate gene transcription by binding to DNA, and can be activated by various compounds.

PGC-1alpha is a transcriptional coactivator of the PPARs that is thought to control adaptive responses to physiological stimuli. PGC-1alpha has been shown to be upregulated with even a single bout of exercise. This increase may play a role in mediating response to exercise, including cardiovascular and metabolic responses. PGC-1alpha has been linked to adaptive thermogenesis, e.g., response to cold, and participates in carbohydrate and lipid metabolism. Fasting has been shown to increase the activity of PGC-1alpha, while insulin has a suppressive effect on PGC-1alpha. PGC-1alpha has also been shown to prevent muscle damage by certain chemical agents.

In accordance with certain embodiments the PPARs and/or the PGC-1alpha compounds or ingredients can be derived or obtained from a natural source such as, for example, a botanical or herbal source. Examples of natural sources of PPARs and/or PGC-1alpha activator compounds, components or ingredients include, but are not limited to, Epimedium sagittatum which is believed to promote PGC-1alpha, PPAR alpha (PPAR-α), and nuclear respiratory factor-1 (NRF-1) expression (i.e., act as an agonist), Epimedium grandiflorum which is believed to promote the expression of PGC-1alpha, PPAR-alpha and NRF-1, and Japanese Knotweed which is believed to be a PGC-1alpha agonist. It is noted that the term “PPAR agonist” as used herein comprises naturally occurring botanical sources that include PPAR activator compounds or components.

In accordance with certain other embodiments, the PPARs and/or the PGC-1alpha compounds or ingredients can be in the form of one or more isolated, purified, or naturally-derived compounds such as, for example, resveratrol which is believed to be a PPAR agonist, piceatannol which is believed to be a PGC-1alpha agonist, sodium pyruvate which is believed to be a PGC-1alpha agonist, and phytanic acid which is believe to be a PPAR-α, PPAR-β, and PPAR-γagonist.

In accordance with certain embodiments, trans-resveratrol, resveratrol derivatives, and resveratrol-related compounds can be included in the nutritional composition as PPAR agonists and to promote or enhance recovery after exercise. Resveratrol has been shown to have many health benefits, including as an anti-inflammatory, blood-sugar regulatory and many cardiovascular benefits.

Piceatannol is the phenolic stilbenoid metabolite of trans-resveratrol which can be found in the seeds of the plant Euphorbia lagascae L. Piceatannol is also known as a natural analog of resveratrol and is believed to be a resveratrol precursor. Piceatannol is further believed to contribute to health benefits such as increased aerobic capacity, improved metabolic homeostasis, and/or improved insulin resistance. Piceatannol may work synergistically with creatine phytanate, phytanic acid, Japanese Knotweed, Rhodiola rosea, Epimedium grandiflorum, Epimedium sagittatum, and/or sodium pyruvate.

Japanese Knotweed (Polygonun cuspidatum) is an herbaceous plant that is a commercial source of resveratrol and is believed to be a PGC-1alpha agonist, an anti-inflammatory agent and acts as a selective estrogen receptor modulator (SERM).

Phytanic acid is a branched-chain fatty acid that is derived from the phytanol side chain of chlorophyll. Phytanic acid is oxidized into pristanic acid. Phytanic acid is believed to be a PPAR-α, β and γ agonist and is also believed to increase nitric oxide production.

In accordance with certain embodiments, the nutritional composition includes one or more PGC-1alpha and PPAR regulating compounds or ingredients in combination with a source of creatine. Suitably, the creatine sources may include salts, esters, derivatives, or conjugates of creatine that further help induce activity of PGC-1alpha and PPARs, such as, for example, creatine heptyl ester, creatine ethyl ester, and the like. Sources of creatine may include creatine salts that act synergistically with other compounds in the invention. Heptanol, heptaminol and heptaminol precursors are contemplated which are anabolic and central nervous system stimulants, and may help increase muscle mass. Another potential creatine source is creatine phytanate, which is believed to improve or enhance strength, endurance and/or muscle size. Other creatine containing salts, solvates, prodrugs, and conjugates are contemplated as useful in the nutritional compositions. Useful creatine containing components include, but are not limited to, creatine monohydrate, Creatine Alpha Amino-N-butyrate, Creatine Ethyl Ester-Beta-Alanine intermixture, Creatinol-O-Phosphate-Malic Acid Interfusion complex, Sodium Creatine Phosphate Matrix, N-phosphatidyl Creatine Heptanoate Ester, Creatine Heptanoate HCl, Ethyl 2-[N-(1-hexadecanaamido-aminomethyl)-N-methylamino]acetate (Creatine Palmitoyl Ethyl Ester HCl), and the like.

In accordance with further embodiments, the nutritional composition can also include an energy source. One suitable energy source is sodium pyruvate which is involved in the cycle that converts glucose to energy (i.e., the Krebs cycle). Enzymes of the Krebs cycle and electron transport chain are located in the mitochondria and it is believed that mitochondrial number and/or improved mitochondrial function may be central to maintaining muscle integrity. Sodium pyruvate has been found to increase the availability of ATP, improve work capacity, and act as a PGC-1alpha agonist. Sodium pyruvate has also been used to promote weight loss.

Another suitable energy source may be in the form of a powder, extract or preparation of Echeveria glauca, a succulent plant from the Crassulaceae family. Echeveria glauca is believed to increase energy metabolism and may also increase glycolytic enzyme production which support anabolism. Another suitable energy source may be Panax gingseng and/or an extract thereof which contains or is enriched in ginsenocides or ginsenosides, a class of steroid glycosides, and triterpene saponins, found exclusively in the plant genus Panax (ginseng).

The nutritional composition can further include one or more anabolic stimulants and/or central nervous system stimulants to help regulate the activity of PPARs to promote anabolism and to act synergistically with other compounds. Examples of suitable anabolic and/or central nervous system stimulants include, but are not limited to hepatanol, heptaminol, L-lyxoflavin, Oxytropis muricata, hydroxyphenethylamine, N-benzoyl-2-hydroxyphenethylamine, and N-nicotinoyl-2-hydroxyphenethylamine.

Heptanol is a saturated primary aliphatic alcohol, also known as heptyl alcohol. Heptanol is a heptaminol precursor, an anabolic and a central nervous system stimulant, and can be found naturally in the careless weed (Amaranthus palmeri) plant. Heptaminol is an amino alcohol that is also classified as a vasodilator. Heptanol may work in synergy with creatine heptyl ester or creatine ethyl ester to further promote the anabolic pathway.

L-lyxoflavin is a synthetic vitamin, which is similar to riboflavin (vitamin B2) except that the d-ribitol is replaced with d-lyxitol. L-lyxoflavin is a steroisomer of riboflavin that is derived from Lyxol. L-lyxoflavin promotes muscle accretion, increases the efficiency of feed utilization, increases growth rate, and is an anabolic vitamin analog.

Oxytropis muricata, hydroxyphenethalamine, N-benzoyl-2-hydroxyphenethylamine and N-nicotinoyl-2-hydroxyphenethylamine are beta-adrenoceptor agonists, anabolic and central nervous system stimulants which are believed to help increase or stimulate muscle growth.

Certain other beneficial compounds and/or natural botanicals, herbs or ingredients may be added to the invention to act synergistically with key ingredients to promote anabolism through the regulation of PPARs, such as PGC-1alpha, or to increase NO production, or for their health benefits. Such beneficial compounds and/or natural ingredients can include, but are not limited to: Rhodiola rosea, rosavin and/or salidroside; Epimedium grandiflorum; Epimedium sagittatum and/or icariin; compounds and/or ingredients which promote protein synthesis and/or increased growth rate such as alpha-hydroxy-isovaleric acid, alpha-hydroxy-isocaproic acid, alpha-hydroxy-beta-valeric acid, Lespedine (kamferol-3,7-dirhamnoside), and/or Shilajit moomiyo extract with fulvic acid and/or humic acid; compounds and/or ingredients which are or contain antioxidants and/or promote improve muscle mass such as kudzu powders, extracts or preparations, robinin, hyperin, and/or hawthorn powders, extracts or preparations; and compounds and/or ingredients which promote insulin sensitivity such as loquat leaf extract and/or maslinic acid.

Rhodiola rosea, a plant in the Crassulaceae family, is an adaptogen and is a natural herb that is known to increase a body's resistance to stress, trauma, anxiety and fatigue. The glycoside compounds Rosavin(s) and salidroside(s) are believed to be responsible for the antidepressant and anxiolytic actions of this plant. Rhodiola rosea is also thought to improve exercise capacity, activate the synthesis of adenosine triphosphate (ATP), act as an anti-inflammatory agent, reduce fatigue and is a PGC-1alpha agonist. Rhodiola rosea is generally used to reduce recovery time after intense workouts. In accordance with certain embodiments, Rhodiola rosea such as in the form of an extract standardized for rosavins and/or salidorsides can be included in the nutritional composition as PPAR/PCG-1alpha agonists and/or as an energy source. In accordance with certain other embodiments, rosavin, salidroside, and/or an alternative botanical source of rosavin and/or salidroside can be included in the nutritional composition.

Epimedium grandiflorum is an herbaceous flowering plant in the family Berberidaceae. The active ingredient in Epimedium grandiflorum is icariin, which is known to increase nitric oxide. Epimedium grandiflorum is also believed to promote the expression of PGC-1alpha, PPAR-alpha and NRF-1.

Alpha-hydroxy-isovaleric acid, alpha-hydroxy-isocaproic acid and alpha-hydroxy-beta-methyl valeric acid are hydroxy acids. All three hydroxy acids have growth promoting capacity, increase protein synthesis and improve recovery time from exercise. Alpha-hydroxy amino acids may also have a standalone anabolic effect. Additional useful hydroxy acids include alpha-hydroxy-gamma-methylthiobutyric acid, alpha-hydroxy-beta-phenylpropionic acid, alpha-hydroxy-beta-imidazolepropionic acid, alpha-hydroxy-beta-hydroxybutyric acid, alpha-hydroxy-gamma-aminocaproic acid, alpha-hydroxy-gamma-guanidinovaleric acid, and the like.

Epimedium sagittatum is an herbal treatment used to increase stamina. Epimedium sagittatum promotes PGC-1alpha, PPAR-alpha, and NRF-1 expression, has antiosteoporotic effects and increases testosterone levels. In accordance with certain embodiments, an Epimedium sagittatum material which has been standardized to include 10% icariin can be included in the nutritional composition. Additionally or alternatively, in accordance with certain other embodiments, icariin or another botanical source of icariin can be included in the nutritional composition.

Kudzu (Pueraria lobata) is a Japanese creeper associated with the legume family. In accordance with certain embodiments, a kudzu material which has been standardized to include 10% robinin can be included in the nutritional composition. Robinin has antioxidant properties and is an anabolic flavonoid. Kudzu materials are also believed to promote increases in muscle mass.

Loquat leaf extract is believed to improve insulin sensitivity, increase protein turnover rate, and stimulate growth. In accordance with certain embodiments, an loquat leaf extract which has been standardized for 10% maslinic acid can be included in the nutritional composition. Olive leaf extract is believed to improve insulin sensitivity, increase protein turnover rate, and stimulate growth. In accordance with certain embodiments, an olive leaf extract which has been standardized for 10% maslinic acid can be included in the nutritional composition.

Hawthorn (Crataegus monogyna) is a hedge plant in the rose family. Active compounds found in hawthorn materials include hyperin (hyperoside), an antioxidant, and various anabolic flavonoids. Hawthorn is also known to be an anti-inflammatory agent and is suspected to help increase muscle mass. In accordance with certain embodiments, the nutritional supplement can include or contain a hawthorn material which has been standardized to include 10% hyperin (Hyperoside).

Shilajit moomiyo is an adaptogenic herb which can be used to enhance physical and mental performance. Shilajit is believed to amplify the benefits of other herbs by enhancing their bio-availability. Shilajit is also believed to increase protein synthesis, growth rate and/or energy intake. Suitably, the nutritional composition can include a Shilajit material or extract which has been standardized to include or contain 10% humic acid and/or 10% fulvic acid. In accordance with certain other embodiments, the nutritional composition can alternatively and/or additionally contain fulvic acid, humic acid, and/or another botanical, natural, or herbal source of fulvic acid and/or humic acid.

The nutritional composition can further include one or more free amino acids including essential amino acids and/or branched chain amino acids. Generally, it has been found that ingesting free amino acids has a beneficial impact on muscle performance and recovery and promotes anabolism. Essential amino acids have generally been shown to have both an anti-catabolic effect and an anabolic effect during exercise and in the post-exercise period while branched chain amino acids (BCAAs), particularly leucine, have been shown to preserve muscle and decrease protein breakdown during times of weight loss or other catabolic circumstances.

Branched chain amino acids consumed during and post workout are thought to spare muscle glycogen, promote anabolism and anti-catabolism, promote recovery, promote alanine and glutamine production, and regulate fatigue (lactic acid) and DOMS (Delayed Onset Muscle Soreness).

Free amino acids which can be utilized in the nutritional composition include, but are not limited to, essential amino acids selected from histidine, methionine, phenylalanine, lysine, threonine, and combinations thereof, and branched chain amino acids (BCAAs) selected from isoleucine, leucine, valine, and combinations thereof, and/or salts, analogues, esters, ethers, and derivatives thereof.

The essential amino acids histidine, methionine, threonine, lysine, phenylalanine, leucine, isoleucine, and valine are amino acids not made by the body and must be consumed from food or supplements. The nutritional composition and methods disclosed herein take full advantage of the ergogenic benefit of combining carbohydrates and essential amino acids.

Additional components or compounds which can be utilized in the nutritional composition include: carbohydrates such as, for example, inulin and/or fructooligosaccharides; effervescent delivery agents such as, for example, bicarbonate compounds; creatine transport aides and/or creatine precursors such as, for example, guanidinopropionic acid, glycocyamine, and/or trimethylglycine (betaine); anti-fatigue agents such as, for example, beta-alanine, PEAK ATP® adenosine 5′ triphosphate (available from TSI Health Sciences, Inc. Missoula, Mont.), and/or creatinol-O-phosphate; electrolytes such as, for example, glycerol stearate and additional sources of calcium, magnesium, potassium, and/or sodium; and excipients such as, for example, calcium silicate, malic acid, and/or citric acid.

The nutritional compositions disclosed herein can be administrated orally as an effective means of regulating athletic function. In addition to peroral use, other routes such as transdermal, sublingual, intranasal, or parenteral, can be used to effectively administer the disclosed nutritional compositions. Other dosage forms and applications include capsules, tablets, caplets, liquids, beverages, liquid capsules, dissolvable films, powders, sprays or functional food products.

Solid nutritional compositions for oral administration in connection with a method for promoting anabolism during exercise may optionally contain, in addition to the above enumerated nutritional composition ingredients or compounds: carrier materials such as corn starch, gelatin, acacia, microcrystalline cellulose, kaolin, dicalcium phosphate, calcium carbonate, sodium chloride, alginic acid, and the like; disintegrators including, microcrystalline cellulose, alginic acid, and the like; binders including acacia, methylcellulose, sodium carboxymethylcellulose, polyvinylpyrrolidone, hydroxypropyl methylcellulose, ethyl cellulose, and the like; and lubricants such as magnesium stearates, stearic acid, silicone fluid, talc, waxes, oils, colloidal silica, and the like. The usefulness of such excipients is well known in the art.

Liquid nutritional compositions for oral administration in connection with a method for promoting anabolism during exercise can be prepared in water or other aqueous vehicles. In addition to the above enumerated ingredients or compounds, liquid nutritional compositions can include suspending agents such as, for example, methylcellulose, alginates, tragacanth, pectin, kelgin, carrageenan, acacia, polyvinylpyrrolidone, polyvinyl alcohol, and the like. The liquid nutritional compositions can be in the form of a solution, emulsion, syrup, gel, or elixir including or containing, together with the above enumerated ingredients or compounds, wetting agents, sweeteners, and coloring and flavoring agents. Various liquid and powder nutritional compositions can be prepared by conventional methods.

As disclosed herein, a method for promoting anabolism during exercise includes orally administering to an individual engaged in exercise or physical activity a nutritional composition comprising at least one PPAR agonist and at least one PGC-1alpha agonist. The nutritional composition can additionally optionally include or contain one or more of: a creatine containing component; an anabolic stimulant; a central nervous system stimulant; a nitric oxide stimulant; an energy source or energy producing agent; a compound that enhances or induces protein synthesis; an antioxidant; an agent to improve insulin sensitivity; and/or compounds that enhance the bioavailability of other ingredients.

Oral daily doses of the nutritional composition can be between about 1 to about 1000 grams, suitably between about 1 to about 100 grams, or, between about 1 to about 30 grams. One exemplary daily dosing schedule can include one serving on training days. In another embodiment, multiple servings can be administered in a day if an individual engages is multiple training sessions (i.e., one dose or serving can be administered during each training session).

The nutritional composition and methods described above may be further understood in connection with the following Example.

Example 1

In accordance with one embodiment, a serving of a nutritional composition can optionally include or consist of the following ingredients:

TABLE 1 Ingredient Function Epimedium sagittatum standardized PPAR and for 10% icariin PGC-1alpha Piceatannol Agonists Epimedium grandiflorum Sodium pyruvate Japanese Knotweed trans-resveratrol Rhodiola rosea extract (root) (3% Rosavins and 1% Salidrosides) Pterostilbene (resveratrol analog) Creatine (including salt or solvate) Sources of Creatine heptyl ester creatine Creatine ethyl ester Creatinol-O-Phosphate N-phosphatidyl heptanoate ester Ethyl 2-[1-N-(hexadecanaamido- aminomethyl)-N-methylamino]acetate (Creatine Palmitoyl Ethyl Ester HCl) Heptanol Anabolic and/or Heptaminol central nervous L-lyxoflavin system stimulants Oxytropis muricata Hydroxyphenethylamine N-benzoyl-2-hydroxyphenethylamine N-nicotinoyl-2-hydroxyphenethylamine Echeveria glauca Energy sources Sodium pyruvate Rhodiola rosea Panax gingseng (Acceleris ®) Alpha-hydroxy-isovaleric acid Protein synthesis/ Alpha-hydroxy-isocaproic acid increased Alpha-hydroxy-beta-methyl valeric acid growth rate Alpha-Hydroxy-Gamma-methylthiobutyric acid Alpha-Hydroxy-Beta-phenylpropionic acid Alpha-Hydroxy-Beta-imidazolepropionic acid Alpha-Hydroxy-Beta-hydroxybutyric acid Alpha-Hydroxy-Gamma-aminocaproic acid Alpha-Hydroxy-Gamma-guanidinovaleric acid Shilajit moomiyo extract with 10% fulvic acid and 10% humic acid Loquat leaf extract standardized for 10% maslinic acid Lespedine (kamferol-3,7-dirhamnoside) Kudzu (Pueraria lobata) standardized for 10% Antioxidant/ robinin improves Hawthorn (Crataegus monogyna) muscle mass standardized for 10% hyperin Lespedine (kamferol-3,7-dirhamnoside) Loquat leaf extract standardized for 10% Improve insulin maslinic acid sensitivity

Acceleris® brand ginseng product is available from Unigen USA, Lacey, Wash.

The nutritional composition as in the above Example is prepared by mixing the components, i.e. chemical and botanical ingredients, in aqueous, lipid, or glycerol solutions. In addition, dried or powder formulations and/or tablets may be prepared. For example, a powder formulation would be an orally deliverable form, which would include the ingredients listed in Table 1, and including a customized flavor system. For example, powder formulations for aqueous suspension are contemplated. Thus, appropriate nutraceutical carriers and excipients comprise liquid, solid, and powder formulations.

Example 2

In accordance with an embodiment, it is expected that a human subject using the nutritional composition of Example 1 by oral administration will show an increase in anabolism after multiple days of use. One expected measure of increased anabolism will be enhanced or increased muscle growth or size. It is also expected that a subject utilizing the nutritional composition of Example 1 will demonstrate enhanced physical performance and/or recovery from fatigue when combined with an established exercise regimen such as repetitive set weight lifting or weight training. One expected measure of enhanced physical performance will be enhanced or increased muscle growth or size. It is expected that total work output will be increased in a subject administered the nutritional composition of Example 1 by oral administration after multiple days of use. Total work output, expressed in units of joules per set, is measured as in U.S. Pat. No. 6,100,287, herein incorporated by reference.

While in the foregoing specification this invention has been described in relation to certain embodiments thereof, and many details have been put forth for the purpose of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain of the details described herein can be varied considerably without departing from the basic principles of the invention.

All references cited herein are incorporated by reference in their entirety. The present invention may be embodied in other specific forms without departing from the spirit or essential attributes thereof and, accordingly, reference should be made to the appended claims, rather than to the foregoing specification, as indicating the scope of the invention. 

1. A nutritional composition comprising at least one PPAR agonist, at least one PGC-1alpha agonist, at least one creatine derivative, and a nutraceutically acceptable carrier.
 2. The nutritional composition of claim 1, wherein the PPAR is PPAR-alpha.
 3. The nutritional composition of claim 2, wherein the at least one PPAR-alpha agonist is selected from one or more of the group consisting of Epimedium sagittatum, Epimedium grandiflorum, and sodium pyruvate.
 4. The nutritional composition of claim 2, wherein the at least one PGC-1alpha agonist is selected from the group consisting of Epimedium sagittatum, Epimedium grandiflorum, sodium pyruvate, piceatannol, Rhodiola rosea, Japanese Knotweed, and combinations thereof.
 5. The nutritional composition of claim 2, wherein the at least one PPAR-alpha agonist and the at least one PGC-1alpha agonist are the same component.
 6. The nutritional composition of claim 1, wherein the creatine derivative is selected from the group consisting of creatine, creatine heptyl ester, creatine ethyl ester, creatinol-O-Phosphate, and a salt or a solvate thereof.
 7. The nutritional composition of claim 6, further including at least one of a component selected from the group consisting of icariin, heptanol, heptaminol, L-lyxoflavin, Oxytropis muricata, hydroxyphenethylamine, N-benzoyl-2-hydroxyphenethylamine, N-nicotinoyl-2-hydroxyphenethylamine, Echeveria glauca, Rhodiola rosea, rosavin, salidroside, Panax gingseng, alpha-hydroxyisovaleric acid, alpha-hydroxyisocaproic acid, alpha-hydroxy-beta-methyl valeric acid, alpha-hydroxy-gamma-methylthiobutyric acid, alpha-hydroxy-beta-phenylpropionic acid, alpha-hydroxy-beta-imidazolepropionic acid, alpha-hydroxy-beta-hydroxybutyric acid, alpha-hydroxy-gamma-aminocaproic acid, alpha-hydroxy-gamma-guanidinovaleric acid, kamferol-3,7-dirhamnoside, Shilajit moomiyo extract, humic acid, fulvic acid, Kudzu (Pueraria lobata), robinin, Hawthorn (Crataegus monogyna), hyperin, Loquat leaf extract, maslinic acid, and mixtures thereof.
 8. A method for increasing anabolism in a human subject during physical activity, the method comprising administering to the subject an effective amount of a nutritional composition comprising at least one PPAR agonist, at least one PGC-1alpha agonist, at least one creatine derivative, and a nutraceutically acceptable carrier, wherein the anabolism of the subject is increased.
 9. The method of claim 8, wherein the effective amount of the nutritional composition is a daily dose from about 1 gram to about 100 grams.
 10. The method of claim 8, wherein the PPAR is PPAR-alpha.
 11. The method of claim 10, wherein the at least one PPAR-alpha agonist is selected from one or more of the group consisting of Epimedium sagittatum, Epimedium grandiflorum, and sodium pyruvate.
 12. The method of claim 10, wherein the at least one PGC-1alpha agonist is selected from the group consisting of Epimedium sagittatum, Epimedium grandiflorum, sodium pyruvate, piceatannol, Rhodiola rosea, and Japanese Knotweed.
 13. The method of claim 8, wherein the creatine derivative is selected from the group consisting of creatine, creatine heptyl ester, creatine ethyl ester, creatinol-O-Phosphate, and a salt or a solvate thereof.
 14. The method of claim 13, wherein the nutritional composition further comprises at least one of a component selected from the group consisting of heptanol, heptaminol, L-lyxoflavin, Oxytropis muricata, hydroxyphenethylamine, N-benzoyl-2-hydroxyphenethylamine, N-nicotinoyl-2-hydroxyphenethylamine, Echeveria glauca, Rhodiola rosea, Panax gingseng, alpha-hydroxyisovaleric acid, alpha-hydroxyisocaproic acid, alpha-hydroxy-beta-methyl valeric acid, alpha-hydroxy-gamma-methylthiobutyric acid, alpha-hydroxy-beta-phenylpropionic acid, alpha-hydroxy-beta-imidazolepropionic acid, alpha-hydroxy-beta-hydroxybutyric acid, alpha-hydroxy-gamma-aminocaproic acid, alpha-hydroxy-gamma-guanidinovaleric acid, kamferol-3,7-dirhamnoside, Shilajit moomiyo extract, Kudzu (Pueraria lobata), Hawthorn (Crataegus monogyna), Loquat leaf extract, and mixtures thereof.
 15. The method of claim 8, wherein the increased anabolism is increased muscle growth.
 16. A method for enhancing physical performance or recovery, the method comprising administering to the subject an effective amount of a nutritional composition comprising at least one PPAR agonist, at least one PGC-1alpha agonist, at least one creatine derivative, and a nutraceutically acceptable carrier.
 17. The method of claim 16, further comprising administering the nutritional composition before, during, or after exercise.
 18. The method of claim 16, wherein the PPAR is PPAR-alpha.
 19. The method of claim 18, wherein the at least one PPAR-alpha agonist is selected from one or more of the group consisting of Epimedium sagittatum, Epimedium grandiflorum, and sodium pyruvate.
 20. The method of claim 18, wherein the at least one PGC-1alpha agonist is selected from the group consisting of Epimedium sagittatum, Epimedium grandiflorum, sodium pyruvate, piceatannol, Rhodiola rosea, and Japanese Knotweed.
 21. The method of claim 17, wherein the creatine derivative is selected from the group consisting of creatine, creatine heptyl ester, creatine ethyl ester, creatinol-O-Phosphate, and a salt or a solvate thereof.
 22. The method of claim 21, wherein the nutritional composition further comprises at least one of a component selected from the group consisting of heptanol, heptaminol, L-lyxoflavin, Oxytropis muricata, hydroxyphenethylamine, N-benzoyl-2-hydroxyphenethylamine, N-nicotinoyl-2-hydroxyphenethylamine, Echeveria glauca, Rhodiola rosea, Panax gingseng, alpha-hydroxyisovaleric acid, alpha-hydroxyisocaproic acid, alpha-hydroxy-beta-methyl valeric acid, alpha-hydroxy-gamma-methylthiobutyric acid, alpha-hydroxy-beta-phenylpropionic acid, alpha-hydroxy-beta-imidazolepropionic acid, alpha-hydroxy-beta-hydroxybutyric acid, alpha-hydroxy-gamma-aminocaproic acid, alpha-hydroxy-gamma-guanidinovaleric acid, kamferol-3,7-dirhamnoside, Shilajit moomiyo extract, Kudzu (Pueraria lobata), Hawthorn (Crataegus monogyna), Loquat leaf extract, and mixtures thereof.
 23. The method of claim 17, wherein said method increases total work output.
 24. The method of claim 17, wherein said method increases muscle growth. 